Canonical Allele Identifier: PA2829654832
Gene: SLC9A6 HGNC NCBI

Linked Data

ClinVar Variation Id: 3165721
ClinVar RCV Id: RCV004457051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006350.1:p.Ala181Ser
CA414749952
NM_006359.3:c.541G>T